环境污染与防治网络版论文摘要

Pb与1,2,4-三氯苯单一及复合污染对蚯蚓毒性机制的研究胡艳祝飞王艳吴石金(浙江工业大学生物与环境工程学院,浙江杭州310014)以赤子爱胜蚓(Eisenia Foetida)作为受试生物,研究了土壤中Pb2+与1,2,4-三氯苯单一及复合污染对蚯蚓的毒性机制。通过滤纸接触法研究Pb2+与1,2,4-三氯苯的单一急性毒性效应,结果表明,两者对赤子爱胜蚓均有毒性。染毒48 h时,Pb2+的半数致死浓     

铜、镉对水螅的急性和联合毒性作用

试验研究重金属铜(Cu2 )、镉(Cd2 )对水螅的急性毒性和联合毒性作用,探索水螅(Hydra sp.)对Cu2 、Cd2 以及两者混合的毒性效应,为水产动物病害的防治中合理使用消毒、杀虫剂以及水体污染评价提供一些参考信息.结果表明,Cu2 对水螅的24 h半致死浓度(LC50)、48 hLC50、72 hLC50、96 hLC50分别为0.072、0.054、0.042、0.037 mg/L;Cd2 对水螅的24 hLC50、48hLC50、72 hLC50、96 hLC50分别为0.001 70、0.000 63、0.000 36、0.000 36 mg/L;Cu2 、Cd2 对水螅的安全浓度分别为3.7×10-4、3.6×10-6mg/L.水螅对两种重金属的毒性反应既快速又敏感,其中Cu2 对水螅的毒性较Cd2 快,但Cd2 的毒性比Cu2 的强.等毒性配比的两种重金属混合液对水螅的毒性大于单一毒性,为协同作用.两种重金属对水螅的LC50随试验时间的延长而减小,它们对水螅的安全浓度远低于渔业水质标准.     

蚯蚓富集猪粪中Cu、Zn的条件优化研究

为探讨利用蚯蚓吸收富集在猪粪中的Cu、Zn以减少其在猪粪中含量的技术途径,实验以赤子爱胜蚓(Eisenia foetida)为生物反应器,采用L18(36)正交设计法,对蚯蚓吸收富集猪粪中Cu、Zn的最适条件进行了研究.结果表明,蚯蚓对猪粪中的Cu、Zn具有一定的吸收能力, 辅料类别、C/N、温度、湿度和蚯蚓密度均能影响蚯蚓对猪粪中Cu、Zn的吸收,综合考虑蚯蚓的生长及对猪粪Cu、Zn的吸收,以猪粪和玉米秸秆为饵料,C/N为22～30、温度为15 ℃、湿度为75%、接种密度为15尾/盆(100 g风干饵料中蚯蚓的生物量为2.29 g)的组合条件下,蚯蚓对猪粪Cu、Zn的吸收总量最高.     

石油污染土壤的生物修复室内模拟实验研究

在实验室模拟的条件下,利用从克拉玛依的石油污染土壤中筛选出的4株高效降解菌,以石油烃降解率、脱氢酶活性、呼吸强度、微生物量碳氮和土壤毒性作为评价指标,研究不加生物菌剂不翻耕、不加生物菌剂翻耕、加生物菌剂不翻耕、加生物菌剂翻耕、加固定化菌剂不翻耕和加固定化菌剂翻耕6种不同实验条件对石油污染土壤修复的效果。结果表明,在63 d的修复过程中,加固定化菌剂翻耕实验F组的石油去除率达到了78.7%,比不加生物菌剂不翻耕实验A组的石油去除率提高了49.5%。随着土壤毒性逐渐降低,玉米(Zea mays L.)和赤子爱胜蚓(Eisenia fetida)可以在F组土壤中良好的生长,达到了修复的效果。     

基于枯草芽孢杆菌的CellSense生物传感器的重金属联合毒性分析

采用聚碳酸醑膜直接固定法制备了基于枯草芽孢杆菌(Bacillus Subtilis)的CellSense生物传感器,分别测定了Cd2+、Cu2+、Zn2+和Cr(Ⅵ)对Bacillus Subtilis的单一毒性,以及等毒性配比和等浓度配比下二元混合体系的联合毒性,并用相加指数法对其联合毒性效应进行了评价.结果表明,基于对数生长后期和稳定期的Bacillus Subtilis的CellSense生物传感器具有良好的毒性分析性能;2种联合毒性评价方法下4种重金属离子二元混合体系的联合作用结果一致,均表现出不同程度的拮抗作用.     

Cu2+和Cr6+对活性污泥处理系统的冲击影响研究

以完全混合活性污泥反应器为试验系统,在作为处理对象的实际餐饮废水中添加Cu2+和Cr6+,分批试验发现添加单一Cu2+的I#系统中,随着Cu2+浓度的增加,污泥浓度及生物相无明显的变化,Cu2+的去除率比较稳定,在90%左右波动;在同时添加Cu2+和Cr6+的Ⅱ#系统中,污泥量明显减少,生物相发生变化,Cr6+浓度达到4.8mg/L,污泥对Cr6+和Cu2+的去除率分别降至27.50%和37.89%.可见,Cr6+对活性污泥系统的毒性远大于Cu2+.     

用水生生物对重金属污染土壤进行生态毒理评价

应用斜生栅藻(Scenedesmusobliquus)和明亮发光杆菌T3(Photobacteriumphosphoreum)急性毒性实验方法对重金属污染土壤的进行生态毒理评价,结果表明,斜生栅藻的生长繁殖率和发光菌的相对发光度与土壤中的重金属含量明显相关,并且随重金属投加量的增加,其生长繁殖率和发光度逐渐降低。对3种测试参数进行比较可知,斜生栅藻细胞数增长率是最敏感的土壤毒性检测指标。土壤的毒性在复合污染的条件下比在单一污染的条件下高很多。本研究的结果可以为污染土壤的优先修复提供理论依据。     

复合污染土壤中十溴二苯醚、铜的同步洗脱

为探究螯合型表面活性剂N-十二酰基乙二胺三乙酸钠盐(LED3A)应用于重金属-十溴二苯醚(BDE209)复合污染土壤洗脱修复的可行性,采用批平衡振荡实验法,研究LED3A对复合污染土壤中Cu和BDE209的同步洗脱效果,考察洗脱时间、洗脱液浓度、pH等对洗脱率的影响.结果表明:LED3A对Cu单一污染土壤、BDE209...     

云南个旧矿区Pb污染稻田土壤钝化修复

针对云南个旧矿区铅污染稻田土壤,研究了复合钝化剂S1(纳米活性炭+硅钾钙镁肥)、S2(火山石+钙镁磷肥+有机肥)和叶面硅肥F单一及联合施用共5种不同调控处理(S1、S2、F、S1+F、S2+F)的田间修复效果及对稻米铅累积的影响。结果表明,5种调控措施对水稻均能产生增产效应,其中两种联合处理(S1+F、S2+F)水稻的增产效果明显优于单一处理(S1、S2、F);经过1个水稻生长周期,5种调控处理土壤pH值较对照均有上升,土壤酸可提取态Pb含量均有降低。与对照相比,S2+F处理水稻增产29.7%,土壤pH上升0.48个单位,土壤酸可提取态Pb降低45.5%,糙米Pb含量降低80.4%、且远低于国家食品卫生标准(GB 2762-2012)。采用复合钝化剂S2(火山石+钙镁磷肥)基施与水稻灌浆期和抽穗期分别喷施叶面硅肥F的土壤钝化-农艺联合调控措施能有效阻控个旧矿区污染土壤中Pb的迁移,降低糙米中Pb的含量,提高矿区稻米安全质量,可在Pb污染农田推广应用。     

复合纳米材料对土壤重金属离子吸持固化的模拟研究

土壤中过量重金属离子可通过食物链和地表水系统危害人群健康。通过土柱淋溶模拟实验,研究了SiO2-Al2O3-Fe2O3等复合纳米材料对土壤溶液中Cu2+、Cd2+、Pb2+、Zn2+和Ni2+的吸持与固化特征。分别向重金属含量4倍于土壤二级标准(GB15618-1995)的土壤中添加0%、4%、6%和10%的复合纳米材料,分析不同深度土壤渗滤液以及土柱上栽培植物不同部位中重金属的含量。结果表明,碱性壤质土壤中重金属向下的迁移量很少;在含4%复合纳米材料土柱中,其吸持固化土壤溶液中63%的Cu、79%的Cd、68%的Pb、89%的Zn和76%的Ni;在含6%复合纳米材料土柱中,其吸持固化土壤溶液中82%的Cu、92%的Cd、76%的Pb、91%的Zn和88%的Ni;再增加土柱中复合纳米材料的含量,其吸持固化效果并不再显著增加。     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Degradation in soil and water and ecotoxicity of rimsulfuron and its metabolites.

The degradation and ecotoxicity of sulfonylurea herbicide rimsulfuron and its major metabolites were examined in batch samples of an alluvial sandy loam and in freshwater. An HPLC-DAD method was adapted to simultaneously identify and quantify rimsulfuron and its metabolites, which was successfully validated by GC-MS analysis. In aqueous solutions, pure rimsulfuron was rapidly hydrolyzed into metabolite 1 (N-(4,6-dimethoxypyrimidin-2-yl)-N-(3-(ethylsulfonyl)-2-pyridinylurea)), which itself was transformed into the more stable metabolite 2 (N-((3-(ethylsulfonyl)-2-pyridinyl)-4,6-dimethoxy-2-pyrimidineamine)), with half-life (t(1/2)) values of 2 and 2.5 days, respectively. Hydrolysis was instantaneous under alkaline conditions (pH = 10). In aqueous suspensions of the alluvial soil (pH = 8), formulated rimsulfuron had a half-life of 7 days, whereas that of metabolite 1 was similar to that in water (about 3.5 days). The degradation of the two major metabolites was also studied in soil suspensions with the pure compounds at concentrations ranging from 1 to 10 mg l(-1). The half-life of metabolite 1 ranged from 3.9 to 5 days, close to the previous values. Metabolite 2 was more persistent and its degradation is strongly dependent on the initial concentration (C0): half-life values ranged from 8.1 to 55 days at 2-10 mg l(-1), respectively. These values are higher than those determined from the kinetics of metabolite 1 transformation into metabolite 2 (t(1/2) = 8-19 days). The ecotoxicity of the three chemicals was evaluated through their effect on Daphnia magna and Vibrio fischeri (Microtox bioassay). No effect was observed on D. magna with 24 and 48 h acute toxicity tests. Similarly, no toxic effect was observed with the Microtox test for the three chemicals in the range of concentrations tested that included the field application dose. Thus, being of low persistence and lacking acute toxicity, these chemicals present a low environmental risk. However, chronic effects should be studied in order to confirm the safety of rimsulfuron and its major metabolites.     

Isocyanatocyclohexane and isothiocyanatocyclohexane levels in urban and industrial areas and possible emission-related activities

Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places.